Transcript EDIT_talk#2x

Excellence in Detectors and Instrumentation Technologies
INFN - Laboratori Nazionali di Frascati, Italy October 20-29, 2015
Application to Medicine & Hadrontheraphy
Lecture#2 - The current status and challenges of
detection and imaging in radiation therapy
Alberto Del Guerra
Functional Imaging and Instrumentation Group
Dipartimento di Fisica “E. Fermi”
Universita’ di Pisa and INFN, Sezione di Pisa
http://www.df.unipi.it/~fiig/
Email:[email protected]
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Contents
–
–
–
–
Rationale for imaging in hadrontherapy
First attempts in the late ‘70s
Proton radiography and proton tomography
Taking advantage of nuclear interactions:
• Modelling
• Positron emitters and PET imaging
• Prompt neutral particles gammas
• Prompt charged particles protons
• Combined systems (INSIDE project)
– A novel technique: PET Cherenkov Imaging
– Conclusions
2
Ionizaton percentage
Advantages of Hadrontherapy

More dose delivered in depth
120
60
Co
100
Protons, 200 MeV
80
60
40
20
00
e5
10
,
8 MeV
15
20
Depth in water (cm)
25
30
Better dose conformation for
the same total dose

Advantage of Hadron-Therapy
Extended Tumor
 Sharp dose fall-off after the Brag Peak




Higher Relative Biological Effectiveness
Highly conformal
More focused on tumor
Max dose at last mm particle’s range (BP)
 Proper spatial superimposition of several Bragg-peaks of different depths and amplitudes,
enables optimal conformation of the delivered dose to the tumor volume.
 The depth of the Bragg Peak depends on the initial energy of the ions, while its width on
the straggling and on the energy spread of the beam has to be small.
11/06/12
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Rationale for imaging in hadrontherapy: critical issues
 CT HU (e.g.calibration apparatus)
 conversion to proton stopping power
 dose calculation uncertainties
Patient related
•RBE values
•Tumor heterogeneity
•Contouring uncertainties
•Reconstruction artifacts in CT
•Machine related
Physics related
•daily positioning on the couch
•internal organ motion
•changes in air cavities
•tumour regression
•weight loss
Other sources
Dose/Bragg Peak
Monitoring is advisable!
Rationale for imaging in hadrontherapy
Planned
.. but there was a tissues variation !!
Dose/Bragg Peak monitoring 2 major techniques
• 1 - Based on X-ray CT- analogous: pCT (only for Protons)
• 2 - Based on Nuclear Reactions of Hadrons in Tissue
•
Off-line & On-line PET
•
Prompt gamma’s and neutrons
•
Prompt charged particles (only for Ions)
6
The BEVALAC experience @Berkeley
with radioactive beams (late‘70s)
“Physical Measurements with High-Energy Radioactive Beams”
A. Chatterjee, W. Saunders, E. L. Alpen, J. Alonso, J. Scherer and J. Llacer
Radiation Research, Vol. 92, No. 2 (Nov 1982), pp. 230-244
Abstract
“Physical measurements were made with high-energy radioactive beams
(positron emitters) produced as secondary particles from a heavy-particle
accelerator. Data are presented for water-equivalent thickness of a silicon
diode,a comparison of Bragg peak ionization depth vs stopping depth,and
differential stopping depths when a beam is intercepted by heterogeneous
materials in the orthogonal direction. A special positron-emitting beam
analyzing (PEBA) system was used to form images of the stopped
radioactive beam. These measurements will have direct impact on chargedparticle radiotherapy,since the precise range of beams of charged particles
to targets within patients can be measured and used for treatment
planning. Also, during the treatments the stopping point of the beam can be
monitored to verify that the treatment is being delivered as planned.
The PEBA detector
IEEE Transactions on Nuclear Science, Vol. NS-26,
No. 1, February 1979, Jorge Llacer, et al.
NaI(Tl) 3” long for the inner; 2” for the outer ones.
In-house electronics+ CAMAC+ and microprocessors
Results: 1 mm resolution – Limited 3-D reconstruction
8
Energy loss distribution with a proton beam of
140.5 MeV in water, using the code PTRAN
(one-dimensional/pencil beam) [1997]
A.Del Guerra et al., “PET Dosimetry in Proton Radiotherapy:a Monte Carlo
Study”, Appl. Radiat. lsot. Vol. 48, No. 10-12, pp. 1617-1624, 1997
Proton radiography and
proton tomography (*)
Using the same particles (i.e. protons) but with a higher
energy, so that they pass through the target:
- Measure the position with a tracker before (upstream) and
after the target (downstream)
- Measure the residual enery with an energy detector
(calorimeter) downstream
- Make one planar view to obtain a proton-radiography (pR)
- Make many projections to obtain a proton-CT (pCT)
(*)The idea was originally proposed by Allan Cormack in 1963
( J.Appl. Phys.1963,34, p.2722)
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Status of the pCT Project
pCT Collaboration (UC Santa Cruz, Loma Linda, Baylor, Wollongong)
UC Santa Cruz, Loma Linda U., Baylor U., Wollongong U.
Tracker:
Extrapolates protons
into the phantom.
4 x-y planes of Silicon
strip detectors with
“slim edges” to avoid
image artifacts.
Energy Detector:
Provides
measurement of the
Water Equivalent Path
Length (WEPL) of the
phantom.
5-stage scintillator with
PMT readout.
http://dx.doi.org/10.1016/j.nima.2015.07.066
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(Courtesy of H.Sadrozinski, 2015)
pCT Collaboration (UC Santa Cruz, Loma Linda, Baylor, Wollongong)
Radiography with pCT Scanner
Wilhelm Roentgen,
Laboratory Radiology (1895)
N.B .
Berta’s hand,
Hand Phantom!
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pCT Collaboration (UC Santa Cruz, Loma Linda, Baylor, Wollongong)
Radiography Relative Stopping Power from X-rays & Protons
X-ray radiograph
transformed from
Hounsfield Units to RSP
Proton Radiograph (directly in
RSP) with 0.5x0.5 mm pixels
About 3%-7%
difference
between X-ray R
and pR
ROI
RSPxray (cm)
RSPproton (cm)
% difference
(2*diff/sum)
a.
3.618±0.130
3.527±0.125
2.55%
0.505σ
b.
2.892±0.070
3.015±0.076
4.16%
1.190σ
c.
4.236±0.119
4.561±0.153
7.39%
1.677σ
d.
2.548±0.082
2.539±0.041
3.54%
0.0981σ
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Relative
Error
pCT Collaboration (UC Santa Cruz, Loma Linda, Baylor, Wollongon)
Testing the RSP Resolution & Dose: CTP 404
The Catphan CTP 404
contains inserts of relative
stopping power varying
from 0.001 to 1.85.
This permits a comparison
of a proton scan with
Geant4 simulation and
X-ray scan.
The reconstructed map of the
relative stopping power
RSP in the CTP 404 phantom
reproduces RSP values of all
inserts with accuracy required
by clinical specifications.
Dose comparison of proton vs. X-ray CT scans:
Using weighted CT Dose Index (CTDI)
Proton CT (2 M histories): CTDI = 0.61 mGy X-ray eq
CBCT:
CTDI = 2.53 mGy
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Taking advantage of
nuclear interactions
Top: proton-nucleus interaction;Bottom:nucleus-nucleus interaction
Ref.: Aafke Kraan, Frontiers in Oncology, 07 July 2015 doi: 10.3389
15
Modelling
A “pletora” of Monte Carlo Codes(*)
FLUKA - <www.fluka.org>
GEANT4 – S.Agostinelli et al. NIM-A, 2003,506(6),250-303
MCNPX/6 -T.Gorley et al. Nucl Techol,2012,180(3),298-315
PHITS -T.Sato et al. Nucl Sci.Techol,2013,50(9),913-923
HIBRAC - L.Silver et al.,Radiat. Meas, 2009,44(1),38-46
SHIELD-HIT – DC Hansen et al.Phys. Med. Biol 2012,57, 2393-409
VMCpro – M.Fippel et al. Med. Phys. 2004,31(8),2263-73
PENELOPEPENH – E.Sterpin et al. Med.Phys. 2013,40.
... and more
(*) - For a thorough discussion see Ref.: Aafke Kraan, “Range verification methods in
particle therapy: underlying physics and Monte Carlo modeling “, Frontiers in
Oncology, 7 July 2015, open access; doi: 10.3389/fonc.2015.00150
Display of stages in nucleon-nucleus
interaction relevant for radiotherapy
Ref.: Aafke Kraan, Frontiers in Oncology, 7 July 2015 doi: 10.3389
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Positron Emitters and PET imaging
p
p
16O
16O
p
15O
n
12C
12C
16O
16O
11C
n
15O
11C
1H:
E = 110
MeV
Target: PMMA
15O, 11C, 13N
10C
12C:
E = 212 AMeV
Target: PMMA
...
15O, 11C, 13N
...
n
• A possible method for the
control of the geometrical
accuracy of the treatment
(TPS) is PET imaging of the
activity generated in the
nuclear interactions in tissue
• Small amounts of β+ emitting radioisotopes
are produced with short half-lives
• 11C (20.3 min)
• 13N (9.97 min)
• 150 (2.03 min)
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18
TERMINOLOGY
(Both for Protons and Carbon)
First pioneer work by W. Enghardt et al. in the ’90 with Carbon
Ions (GSI/Bastei tomograph)
• Off-line PET (e.g.) (MGH/Heidelberg/CHIBA)
HoweverIn-beam/In-room dedicated instruments are needed to:
1- Avoid patient re-positioning
2- Avoid data loss of very short living isotopes (e.g. 15O )
3- Avoid radioisotope wash-out
• On-line PET (only on phantoms up until now)
In Room-PET, but off-Beam
(GSI/PISA-CNAO/CHIBA/MGH/HEIDELBERG)
In Beam-PET, but with beam-on
(PISA-CNAO/CHIBA-openPET)
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Rationale
for “
PET monitoring
(Dose  Activity: Standard Approach)
 Comparison between simulated and measured activity with PET
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PET monitoring (Dose Activity: The “Filtering”)
Rationale
 From the planned dose the simulated activity profile is obtained by using the
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filter approach (ref.:F.Attanasi, et al. Phys. Med. Biol, 2011, 56, 5079-5098).
PET monitoring : The dream
 The delivered dose is measured from the measured activity of PET by using an inverse
filtering .The planned dose can then be compared with the measured dose
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DoPET(University of PISA & INFN)
DoPET is a stationary 2 heads tomograph
- gantry compatibility
- in-beam acquisition
15x15 cm2
9 modules
per head
15x15 cm2
DoPET (9 vs 9 modules)
The current prototype is an upgrade of a previous 4x4 system
S,Vecchio, IEEE Trans. Nucl. Science, 56 (1), (2009)
G.Sportelli, IEEE Trans. Nucl. Science 58 (3) (2011)

Hardware (9x9 modules)
- Each detecting module made of
one LYSO matrix (23 x 23 crystals, 2mm pitch)
one PS-PMT 8500 Hamamatsu
Dedicated front-end electronics
- FPGA based acquisition and coincidence processing
(Coincidence time window ~5 ns).
•
Software: Activity reconstruction algorithm:
- Maximum Likelihood Estimation Maximization (MLEM)
- The reconstruction is performed in few minutes
We are working on implementing GPU for bringing
down the time to 30s
Protons and Carbon ions onto PMMA phantoms:
Imaging of the produced activity
Proton beam
98 MeV
z
r(g/cm**3)
H(%)
C (%)
O (%)
PMMA
1.18
8
60
32
H2O
1.0
11.19
88.81
Carbon beam
178 MeV/u
z
heads
distance 30cm
z
y
y
y
FLUKA MC
z
FLUKA MC
z
Protons 2Gy
(TPS-Single fraction)
Two cavities z-profiles
Acquisition time:0-600 s
Difference: full vs. void
exp ~ 4 mm
MC ~ 3mm
10mm
cavity
140 mm
Reproducibility: void vs. void
phantom
entrance
surface
z
z
Prompt gamma’s w/protons
Measurements with collimated detectors
moving
target
Energy spectrum 160 MeV protons in
PMMA, NaI(Tl) detector
beam
collimator
detector
Energy: <1 MeV to 10 MeV
Smeets
A small fraction is measured as discrete lines
Low energy gammas: larger scattered fraction
Synchronization with accelerator RF or monitor and Time of Flight
PMB 2012
D.Dauvergne AAPM 2014
27
Nuclear fragmentation w/C-12 Ions
• Dose deposition during radiotherapy:
– Ionization (in black on the plot)
• Hadrontherapy:
– Nuclear fragmentation
• High probability
• Influence on dose deposition
• Secondary particles
GEANT4
– g, n, p, fragments
– Radioactive Isotopes (b+)
– Range control by means of
nuclear reaction products:
– Prompt gamma’s
≤ 1 per nuclear reaction
~ isotropic emission
Massive particle background (p,n)
D.Dauvergne AAPM 2014
28
Prompt gamma’s measurements
110 MeV protons in water
J.Verburg, PMB 2013
PG yield above 1 MeV
~ 0.3% /cm per proton
~ 2% /cm per carbon
95 MeV/u carbon ions in PMMA
M. Pinto et al, Med Phys 2015
High resolution profiles: influence
of heterogeneities close to the
Bragg peak
D.Dauvergne AAPM 2014
29
Detectors for Prompt gamma’s
Collimated cameras
• Multi-slit cameras
–
–
–
–
Seoul
Lyon ~1mm at pencil beam scale (108 protons)
Delft - Multislit with TOF (project)
MGH: TOPAS Simulation of collimated camera for passive delivery:
Synchronization with range modulator wheel (M. Testa, PMB 2014, J.
Verburg, PMB 2015)
• Knife edge
– Seoul (D. Kim, JKPS 2009)
– Delft : Simulation (Bom, PMB 2012, Cambraia Lopes, PMB 2015)
– IBA : Operational prototype (Perali, PMB 2014, Preignitz, PMB 2015)
Compton cameras
–
–
–
–
No collimation: potentially higher efficiency
Potentially better spatial resolution (< 1cm PSF)
If beam position known  simplified reconstruction
3D-potential imaging (several cameras)
D.Dauvergne AAPM 2014
30
Compton camera
Lyon project: TOF and beam position with hodoscope
Count rate issue
Simulation: line-cone reconstruction for Lyon prototype
1 distal spot (108 incident protons) incident on PMMA target, 160 MeV
Continuous beam (IBA C230)
Clinical intensity: 200 protons/bunch S/N=1/10
Reduced intensity: 1 proton/bunch S/N=5/1
(J.Krimmer, NIMA 2015)
D.Dauvergne AAPM 2014
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Prompt protons
Charged fragments - large angles
• Tracks reconstructed by the Dose CHarged
particle profile (DCH)
beam
direction
➡ Detector
alignment done with aluminum table
fixed positions (± 1mm)
φ = 60°
➡ DCH
center aligned with fixed BP positions
(xPMMA = 0, ~1.5 cm before exit window)
➡Ω
~ 6⋅10-5 sr, εdet > 90%
➡ DCH
trk resolution @ emission point ~ 1mm
He
beam
@90°
12C
Mostly
p,d,t
Mostly
p,d,t
data
(Courtesy of V.Patera, 2015)
beam
data
@90°
data
Bragg Peak monitoring on He beams
particles at large angles is observed for
all beam types
Y (cm)
• A non negligible production of charged
data
BP
• The emission shape is correlated to the
He 145
He 125
He 102
beam entrance window and BP position
as already measured with 12C
Beam type/E
φ 90° (10-3)
He 102
0.6
He 125
0.7
He 145
1
C 160
1
C 180
2
C 220
3
O 210
3
O 260
5
O 300
10
# of tracks/0.4 cm
• φ = dNall/(Nions dΩ)
data
Z
proj.
Z (cm)
BP
different PMMA thickness !!
He 145
He 125
He 102
Z (cm)
33
(Courtesy of V.Patera, 2015)
INnovative Solutions for In-beam
DosimEtry in Hadrontherapy
Pisa,Torino,Roma”La Sapienza”,Bari,INFN
INSIDE coordinator: M. G. Bisogni (Pisa)
This project has been supported by Italian MIUR under the
program PRIN 2010-2011 project nr. 2010P98A75 and by EU FP7
for research, technological development and demonstration under
grant agreement no 317446 (INFIERI)
N. Belcari
N. Marino
N. CamarlinghiM. Morrocchi
A. Del Guerra M.A. Piliero
S. Ferretti
G. Pirrone
E. Kostara
V. Rosso
A. Kraan
G. Sportelli
B. Liu
partners:
P. Cerello C. Peroni
S. Coli
A. Rivetti
E. Fiorina R. Wheadon
G. Giraudo A. Attili,
F. PennazioS. Giordanengo
E. De Lucia
V. Patera
R. Faccini
L. Piersanti
P.M. FrallicciardiA. Sarti
M. Marafini
A. Sciubba
C. Morone
C. Voena
F. Ciciriello
F. Corsi
F. Licciulli
C. Marzocca
G. Matarrese
G.
Battistoni
M.
Cecchetti
F.
Cappucci
S. Muraro
P. Sala
The
Prompt secondary
particles emission
DOSE PROFILER
Project
b+ activity
distribution
IN-BEAM
PET HEADS
Tracker +
Calorimeter =
BI-MODAL MONITORING
SYSTEM
Goals:
 To be integrated in the
gantry
 To be operated in-beam
 To provide an
IMMEDIATE feedback
on the particle range
@
In-beam PET heads
10x 20 x 5 cm3
Distance from the
isocenter=25 cm
256 LFS pixel crystals (3x3x20mm3) coupled one to one
to MPPCs (Multi Pixel Photon Counters, SiPMs).
phantom
Demonstrator
1 vs 1 module
Tested at CNAO
On May 5 2015
Solid
model
Of the PET
head
Work partly supportedd by the European Union EndoTOFPET-US project and by a Marie Curie
Early Initial Training Network Fellowship of the European Union 7th Framework Program (PITNGA-2011-289355-PicoSEC-MCNet).
PET modules
Mono-energetic proton beams
PET reconstructed activity
inter-spill
p beam
p beam
in-spill
after treatment
b+ activity distribution
can be determined
both in-spill,
Inter-spill and after
few minutes of
Irradiation
p beam
The MC simulation is a
reliable tool to evaluate
the performance of the
full in-beam PET
system.
Dose Profiler
Elettronics: BASIC32, FPGA
water cooling
28 x 28 x 35 cm3
6 planes of orthogonal squared
scintillating fibers coupled to SiPMs
 an electromagnetic calorimeter
coupled to Position Sensitive PMTs.

6 fibre planes
X,Y (500 μm)
fibers
plastic
scintillator
multi anode
PMTs
calorimeter
INSIDE: a combined system x protons and x Ions
:
b+ activity detection:
IN-BEAM PET HEADS
 secondary particle tracking:
DOSE PROFILER
to provide 3D real-time monitoring in hadrontherapy

MC simulation is essential for system design, development and operation
In-beam PET: two-steps technique reduces the simulation time (70x),
validated on real data
Dose Profiler: secondary particle signal quantification with 12C beam
In-beam PET first modules (tested at CNAO, May 2015):

very satisfactory results

both in-spill and inter-spill and off beam. PET imaes

adequate coincidence time resolution
The commissioning of the INSIDE system
at CNAO is planned by early 2016.
Contacts: Maria Giuseppina Bisogni [email protected]
A novel technique :
PET Cherenkov Imaging
40
Čerenkov Effect (1934)




Emission of bluish-white light
when a charged particle travels
in a dielectric medium with a
velocity greater than the speed
of light in that medium ⇒
threshold process
Instantaneous emission (no
delay like scintillation)
Emission dependent on medium
refractive index (the higher the
better, but everything with n > 1
can shine!)
Continuous spectrum (∝ 1/λ2)
limited by medium window of
transparency
Čerenkov Luminescence Imaging (CLI)
Beta decay products in tissue are charged
particles in dielectric medium ⇒ Čerenkov
emission associated with beta decay
 Beta spectrum determines light production:
18F → 2 Č/decay, 90Y → 70 Č/decay (Mitchell 2011)
 Faint signal, strong absorption and scattering
(max path 1-2 cm)
 β- imaging, ease of use, $$$$

Small animal CLI: state of the art
Spinelli et al. 2010, San
Raffaele and University of
Verona - 18F-FDG uptake
(a) CLI image 1 h after 18F-FDG
injection
(b) 18F-FDG average radiance from
heart, bladder and background
regions in the animal during the
first hour after 18F-FDG injection.
Li et al, 2010 UC Davis –
Čerenkov luminescence
tomography (CLT)
using spectral
acquisitions and
multiple views acquired
with mirrors
Small animal CLI: state of the art
Holland et al, 2011 MSKCC Intraoperative CLI during
surgical resection
Thorek et al, 2013 MSKCC - Excitation of fluorofores with Čerenkov radiation (SCIFI)
Can CLI be quantitative?
Liu et al, 2012 Stanford – cross-calibration with PET
In vivo CLI and PET
images of mice bearing
tumour.
(A)
(B) Corresponding relative
quantitative analysis of CLI and
PET results and their correlation.
Cerenkov (Based) PET imaging
20-25 cm axial  Patient bed motion
Step and shoot or continuous motion
for a full body image
Snap-shot for a full body
The annihilation quanta (511 keV) interact via Compton scattering or
photoelectric effect in the detector material. Materials with high density and high
atomic number are advantageous, because the chance for interaction is higher,
with a large fraction being photoelectric absorption. In either case,
energy is transferred to an electron. If energy transfer is sufficiently high,
Cherenkov light is emitted while the electron is travelling through the material. By
measuring Cherenkov light, the gamma ray interaction is detected.
Cerenkov (Based) PET imaging
• Develop a PET-detector based on a Cherenkov radiator with spatial
resolution of about 4 mm and 100 ps coincidence timing resolution.
This includes radiator material and light sensor.
•
Develop a scalable, fast readout electronics enabling parallel
acquisition of more than 100,000 individual detection channels.
• Develop data processing and image reconstruction methods which
make use of the unique features of Cherenkov-PET, such as
intrinsic gamma energy selection, 100 ps TOF, and individual
readout of detection elements.
• Optimize system parameters aiming at a full-body
Cherenkov-PET tomograph.
CONCLUSIONS
48
Take Home Message #1
• MULTIMODALITY is the PRESENT:
– PET/CT
– PET/MR
– PET/OPT,Cherenkov
– and more…
• PET organ/application specific is the FUTURE:
– Brain
– Breast
– Prostate
– Hadrontherapy
– and more…
49
Take home message #2
years
Consumer cycle: 3 y
•
•
Medical device cycle 15-20 y
Technology Transfer in the medical field needs
long term investment
Industry can withdraw half-way through, if not
profitable,e.g. Siemens for proton therapy
Ref: From the keynote talk by Dr. Jaemoon Jo
(SamsungSenior Vice-President) at MIC_2013, Seoul
Suggested Further Readings
“Ionizing Radiation Detectors for medical imaging”,
World Scientific , 2004. Alberto Del Guerra.“ ISBN 981238-674-2
“Positron Emission Tomography- Basic Science and
Clinical Practice”, Springer,2003, P. Valk,
D.L:Bailey,D.W.Townsend, M.N.Maisey, ISBN: 1-85233485-1
“Medical Imaging-Technology and Applications”, CRC
Press, 2014.Edited by Troy Farncombe and Krzysztof
Iniewski, ISBN 978-1-4665-8262
“Webbs’s Physics of Medical Imaging,” Second
edition, CRC Press, 2012, Edited by M A Flower, ISBN:
978-0-7503-0573-0
Ackowledged contributions from:
Harmut Sadrozinski (UC Santa Cruz, USA)
Denis Dauvergne (in2p3, France )
Vincenzo Patera (University of Roma “La Sapienza”)
... and more
... and the members of the Fiig Group (Pisa University),
in particular:
Valeria Rosso
Maria Giuseppina Bisogni
THANK YOU!
Questions?
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